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. 2011 Aug;193(15):3912–3922. doi: 10.1128/JB.00386-11

Table 1.

Oligonucleotide primers used in this study

Primer Sequence (5′ → 3′)a Commentb
P1 GACAGTTTACTCGGCACG Flanking region before TDE0143; F
P2 ATCGATCAGCCCTTTGCGGGTATG Flanking region before TDE0143; R
P3 ATCGATCTCAAAGCCTCCTTCCCG Flanking region after TDE0143; F
P4 AGATATTTCGGTGAGGGC Flanking region after TDE0143; R
P5 ATCGATCCGATAGCTTCCGCTATTGC erm cassette; F
P6 ATCGATGGAAGCTGTCAGTAGTATACC erm cassette; R
P7 CGGAGAAGCTCCCATAGC Co-RT-PCR, TDE0143-TDE0144; F
P8 AAAGATGAGGCCGCCGAG Co-RT-PCR, TDE0143-TDE0144; R
P9 CCCATGTGCAAGAAGGGC Co-RT-PCR, TDE0144-TDE0145; F
P10 GACCATTCCGATTCCGCG Co-RT-PCR, TDE0144-TDE0145; R
P11 CATTACCCCTCTTGTCGAG Co-RT-PCR, TDE0145-TDE0146; F
P12 CGTTAATCTCGGCTATACC Co-RT-PCR, TDE0145-TDE0146; R
P13 CACCTGTGCCGCTCTTTTTGCA rTbpATd; F
P14 CTAAGCAAGTCCCTTGATAAC rTbpATd; R
P15 GAATTCGGACAACTTGTTATTATGCAC 5′ of tbpATd thi-box; F
P16 GGATCCTGCAAAAAGAGCGGCACAACC 3′ of tbpATd thi-box-L; R
P17 GGATCCCATATGCTCCCTCCGCCGGTA 3′ of tbpATd thi-box-S; R
P18 TAATTATCGGTTGTGCCGCT TDE0143 5′-RACE sensor primer; F
P19 CGGCAATACCCATACCTTCA TDE0143 5′-RACE inner primer; R
P20 TGCAGGTTTGGGAACATCCT TDE0143 5′-RACE outer primer; R
P21 CTGACGGAACAAAGGTTGTAG qRT-PCR, TDE0143; F
P22 CCTTACCTTCCAGTATGACTC qRT-PCR, TDE0143; R
P23 TAGGATTGCTGCCTTTACGG qRT-PCR, TDE0144; F
P24 ATTATTGCAGGCACGCAGAG qRT-PCR, TDE0144; R
P25 TCAGGCTGCGGCAAAACAAC qRT-PCR, TDE0145; F
P26 CATTGAGATGAGGGAAGAGG qRT-PCR, TDE0145; R
P27 CCGTCCATTGTAGGCTTTAC qRT-PCR, dnaK; F
P28 CCGTCAATGTCGATTCGTAC qRT-PCR, dnaK; R
P29 TGCTTTTACAAGCTAAAAACATACCCGCAA TPP-binding site mutagenesis; F
P30 TTGCGGGTATGTTTTTAGCTTGTAAAAGCA TPP-binding site mutagenesis; R
P31 GCAGCACATCCCCCTTTC qRT-PCR, lacZ; F
P32 CGTTGGTGTAGATGGGCG qRT-PCR, lacZ; R
P33 AACGTACTGGCAGATGCAG qRT-PCR, groEL; F
P34 GCGCTTTCAGTTCTTCAACTG qRT-PCR, groEL; R
a

The engineered restriction enzyme sites are underlined.

b

F, forward primer; R, reverse primer.